Enzymatic in vitro reduction of ketones VI. (1) reduction rates and stereochemistry of the HLAD-catalyzed reduction of 3-alkyl- and 4-alkylcyclohexanones
Author:
Publisher
Wiley
Subject
General Chemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/bscb.19800890209/fullpdf
Reference27 articles.
1. Enzymatic “In Vitro” Reduction Of Ketones. V. (1) Reduction of 1-alkyl-4-piperidones in an ethanol - NAD+ - HLAD - system
2. Enzymatic “in vitro” reduction of ketones. IV. (1) Preparative scale reductions of cyclohexanone derivatives in an ethanol-NAD+-HLAD system.
3. Enzymatic “in vitro” Reduction of ketones. I. Kinetics of coupled-substrate coenzyme recycling systems
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1. Continuous-Flow Biocatalytic Process for the Synthesis of the Best Stereoisomers of the Commercial Fragrances Leather Cyclohexanol (4-Isopropylcyclohexanol) and Woody Acetate (4-(Tert-Butyl)Cyclohexyl Acetate);Catalysts;2020-01-10
2. Enzymatic “in Vitro” Reduction of Ketones: Part 9. Preparation of Pure (1S, 2S)-2-Chlorocyclohexanol;Bulletin des Sociétés Chimiques Belges;2010-09-01
3. Enzymatic “In Vitro” Reduction of Ketones VII.(1) Reduction rates and stereochemistry of the HLAD catalyzed reduction of 2-alkyl cyclohexanones, dimethyl cyclohexanones, cycloalkanones and bicycloalkanones;Bulletin des Sociétés Chimiques Belges;2010-09-01
4. Enzymatic “in vitro” reduction of ketones Part 10 (1). Study of 3-Acetylpyridine Adenine Dinucleotide in a Co-enzyme Recycling System Ethanol-Ketone-3-AcPyAD+-HLAD;Bulletin des Sociétés Chimiques Belges;2010-09-01
5. Modelling the Substrate Binding Domain of Horse Liver Alcohol Dehydrogenase, HLADH, by Computer Aided Substrate Overlay;Structure and Chemistry (Part D);1995
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